CO Desorption Rate Dependence on CO Partial Pressure over Platinum Fuel Cell Catalysts

被引:52
作者
Davies, J. C. [1 ]
Nielsen, R. M. [1 ]
Thomsen, L. B. [1 ]
Chorkendorff, I. [1 ]
Logadottir, A. [2 ]
Lodziana, Z. [2 ]
Norskov, J. K. [2 ]
Li, W. X. [4 ]
Hammer, B. [4 ]
Longwitz, S. R. [3 ,5 ]
Schnadt, J. [3 ,5 ]
Vestergaard, E. K. [3 ,5 ]
Vang, R. T. [3 ,5 ]
Besenbacher, F. [3 ,5 ]
机构
[1] Tech Univ Denmark, Dept Phys, Dept Chem Engn, Interdisciplinary Ctr Catalysis ICAT, DK-2800 Lyngby, Denmark
[2] Tech Univ Denmark, Dept Phys, Ctr Atom Scale Mat Phys CAMP, DK-2800 Lyngby, Denmark
[3] Univ Aarhus, Interdisciplinary Nanosci Ctr, DK-8000 Aarhus C, Denmark
[4] Univ Aarhus, Inst Phys & Astron, DK-8000 Aarhus C, Denmark
[5] Univ Aarhus, Dept Phys & Astron, DK-8000 Aarhus C, Denmark
基金
新加坡国家研究基金会;
关键词
Co-Tolerance; Ligand Effect; PEM Fuel Cell; Platinum; Ruthenium;
D O I
10.1002/fuce.200400046
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Carbon monoxide adsorption on high area platinum fuel cell catalysts was investigated. Isotopic exchange experiments were performed to determine the exchange rate (k) of CO under different partial pressures of CO (p(CO)) in argon. A linear dependence of In(k) with In(p(CO)) was observed. This pressure dependence of the rate of exchange is explained by considering a change in surface coverage of CO with different CO pressures and a subsequent reduction in the CO binding energy as demonstrated by Density Functional Theory (DFT) calculations. High Pressure Scanning Tunneling Microscopy (HP STM) studies on the Pt(111) surface have also displayed a pressure dependency of the coverage consistent with this data. The relevance of these observations to the Polymer Electrolyte Membrane Fuel Cell (PEMFC) anode reaction is discussed.
引用
收藏
页码:309 / 319
页数:11
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